化学
己内酰胺
氨基酸
选择性
结构-活动关系
磺胺
立体化学
药理学
生物化学
体外
有机化学
医学
催化作用
作者
Martin L. Neitzel,Danielle L. Aubele,Jennifer L. Marugg,Jacek Jagodziński,Andrei W. Konradi,Michael A. Pleiss,Balázs Szőke,Wes Zmolek,Erich Goldbach,Kevin P. Quinn,John‐Michael Sauer,Elizabeth F. Brigham,William H. Wallace,Michael P. Bova,Susanna S. Hemphill,Guriqbal S. Basi
标识
DOI:10.1016/j.bmcl.2011.04.079
摘要
Herein we describe the structure-activity relationship (SAR) of amino-caprolactam analogs derived from amino-caprolactam benzene sulfonamide 1, highlighting affects on the potency of γ-secretase inhibition, selectivity for the inhibition of APP versus Notch processing by γ-secretase and selected pharmakokinetic properties. Amino-caprolactams that are efficacious in reducing the cortical Aβ(x-40) levels in FVB mice via a single 100 mpk IP dose are highlighted.
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